TY - JOUR
T1 - Electrospun Matrices for Pelvic Floor Repair
T2 - Effect of Fiber Diameter on Mechanical Properties and Cell Behavior
AU - Vashaghian, Mahshid
AU - Zandieh-Doulabi, Behrouz
AU - Roovers, Jan Paul
AU - Smit, Theodoor Henri
N1 - Publisher Copyright: © 2016, Mary Ann Liebert, Inc.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Electrospun matrices are proposed as an alternative for polypropylene meshes in reconstructive pelvic surgery. Here, we investigated the effect of fiber diameter on (1) the mechanical properties of electrospun poly (lactic-co-glycolic acid)-blended-poly(caprolactone) (PLGA/PCL) matrices; (2) cellular infiltration; and (3) the newly formed extracellular matrix (ECM) in vitro. We compared electrospun matrices with 1-and 8 μm fiber diameter and used nonporous PLGA/PCL films as controls. The 8-μm matrices were almost twice as stiff as the 1-μm matrices with 1.38 and 0.66 MPa, respectively. Matrices had the same ultimate tensile strength, but with 80% the 1-μm matrices were much more ductile than the 8-μm ones (18%). Cells infiltrated deeper into the matrices with larger pores, but cellular activity was comparable on both substrates. New ECM was deposited faster on the electrospun samples, but after 2 and 4 weeks the amount of collagen was comparable with that on nonporous films. The ECM deposited on the 1-μm matrices, and the nonporous film was about three times stiffer than the ECM found on the 8-μm matrices. Cell behavior in terms of myofibroblastic differentiation and remodeling was similar on the 1-μm matrices and nonporous films, in comparison to that on the 8-μm matrices. We conclude that electrospinning enhances the integration of host cells as compared with a nonporous film of the same material. The 1-μm matrices result in better mechanical behavior and qualitatively better matrix production than the 8-μm matrices, but with limited cellular infiltration. These data are useful for designing electrospun matrices for the pelvic floor.
AB - Electrospun matrices are proposed as an alternative for polypropylene meshes in reconstructive pelvic surgery. Here, we investigated the effect of fiber diameter on (1) the mechanical properties of electrospun poly (lactic-co-glycolic acid)-blended-poly(caprolactone) (PLGA/PCL) matrices; (2) cellular infiltration; and (3) the newly formed extracellular matrix (ECM) in vitro. We compared electrospun matrices with 1-and 8 μm fiber diameter and used nonporous PLGA/PCL films as controls. The 8-μm matrices were almost twice as stiff as the 1-μm matrices with 1.38 and 0.66 MPa, respectively. Matrices had the same ultimate tensile strength, but with 80% the 1-μm matrices were much more ductile than the 8-μm ones (18%). Cells infiltrated deeper into the matrices with larger pores, but cellular activity was comparable on both substrates. New ECM was deposited faster on the electrospun samples, but after 2 and 4 weeks the amount of collagen was comparable with that on nonporous films. The ECM deposited on the 1-μm matrices, and the nonporous film was about three times stiffer than the ECM found on the 8-μm matrices. Cell behavior in terms of myofibroblastic differentiation and remodeling was similar on the 1-μm matrices and nonporous films, in comparison to that on the 8-μm matrices. We conclude that electrospinning enhances the integration of host cells as compared with a nonporous film of the same material. The 1-μm matrices result in better mechanical behavior and qualitatively better matrix production than the 8-μm matrices, but with limited cellular infiltration. These data are useful for designing electrospun matrices for the pelvic floor.
KW - Electrospinning
KW - PCL
KW - PLGA
KW - PLGA/PCL
KW - fiber diameter
KW - myofibroblastic differentiation
KW - reconstructive pelvic surgery
KW - tissue regeneration
UR - http://www.scopus.com/inward/record.url?scp=85006078180&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85006078180&partnerID=8YFLogxK
U2 - https://doi.org/10.1089/ten.tea.2016.0194
DO - https://doi.org/10.1089/ten.tea.2016.0194
M3 - Article
C2 - 27676643
SN - 1937-3341
VL - 22
SP - 1305
EP - 1316
JO - Tissue Engineering - Part A
JF - Tissue Engineering - Part A
IS - 23-24
ER -